Publications by authors named "J Kevin Donahue"

Purpose: Glioblastoma (GBM) that presents as leptomeningeal disease (LMD) is extremely rare and fatal. Limited data are available regarding incidence, clinical presentation, and management. Prognosis is poor and no treatment is known to improve survival.

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Inositol pyrophosphates are eukaryotic signaling molecules that have been recently identified as key regulators of plant phosphate sensing and homeostasis. Given the importance of phosphate to current and future agronomic practices, we sought to design plants, which could be used to sequester phosphate, as a step in a phytoremediation strategy. To achieve this, we expressed diadenosine and diphosphoinositol polyphosphate phosphohydrolase (DDP1), a yeast (Saccharomyces cerevisiae) enzyme demonstrated to hydrolyze inositol pyrophosphates, in Arabidopsis thaliana and pennycress (Thlaspi arvense), a spring annual cover crop with emerging importance as a biofuel crop.

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Glioblastoma (GB) is a highly heterogeneous type of incurable brain cancer with a low survival rate. Intensive ongoing research has identified several potential targets; however, GB is marred by the activation of multiple pathways, and thus common targets are highly sought. The signal regulatory scaffold IQGAP1 is an oncoprotein implicated in GB.

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Article Synopsis
  • Rare cases of Alzheimer's disease (AD) pathology can sometimes present as parkinsonism, but these occurrences as initial symptoms of AD are not frequently reported.
  • A clinical case study showed that a patient had symptoms resembling idiopathic Parkinson's disease for 12 years, with dementia emerging 6 years after the initial PD diagnosis.
  • Neuropathological examination revealed changes consistent with Alzheimer's rather than Parkinson's disease, with findings like neurofibrillary tangles and amyloid plaques suggesting that AD pathology could explain the patient's parkinsonism symptoms.
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  • * Novel therapies, particularly gene therapy, are being explored to address the underlying mechanisms of AF, using specific genes and delivery methods to target structural changes that increase the risk of this arrhythmia.
  • * This review will cover the essential components of gene therapy for AF, including potential molecular targets, methods for delivering genes to the heart, and insights from early testing on effectiveness and safety, while also discussing recent advancements and ongoing challenges in the field.
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